A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4747449



Internal ID20523467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:33083097..33083166hg38UCSC Ensembl
chr19:33574003..33574072hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16296301
Samples
Known GenesGPATCH1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4747449
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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